Canonical Allele Identifier: PA2830323050
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 1782887
ClinVar RCV Id: RCV002410920
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_696996.1:p.Thr36Ala
CA398271080
NM_153321.3:c.106A>G